Canonical Allele Identifier: PA916056568
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13335
ClinVar RCV Id: RCV000014263 RCV000037663 RCV000077862 RCV000190417 RCV000458650 RCV001376066 RCV001813200 RCV004532343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Phe285Ser
CA204408
NM_080601.3:c.854T>C